Cellular basis for arrhythmogenesis in an experimental model of the SQT1 form of the short QT syndrome (Q34764296)

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4 January 2020

title

Cellular basis for arrhythmogenesis in an experimental model of the SQT1 form of the short QT syndrome (English)

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4 January 2020

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2

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4 January 2020

Charles Antzelevitch

series ordinal

3

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4 January 2020

author name string

Chinmay Patel

series ordinal

1

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publication date

29 January 2008

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4 January 2020

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4 January 2020

volume

5

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issue

4

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4 January 2020

page(s)

585-590

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Role of spatial dispersion of repolarization in inherited and acquired sudden cardiac death syndromes.

4 January 2020

cites work

1 reference

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Reduction of dispersion of repolarization and prolongation of postrepolarization refractoriness explain the antiarrhythmic effects of quinidine in a model of short QT syndrome

7 July 2018

1 reference

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Loss-of-function mutations in the cardiac calcium channel underlie a new clinical entity characterized by ST-segment elevation, short QT intervals, and sudden cardiac death

7 July 2018

1 reference

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Short QT syndrome: a case report and review of literature

7 July 2018

1 reference

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Short QT syndrome: clinical findings and diagnostic-therapeutic implications

7 July 2018

1 reference

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Amplification of spatial dispersion of repolarization underlies sudden cardiac death associated with catecholaminergic polymorphic VT, long QT, short QT and Brugada syndromes

7 July 2018

1 reference

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Short QT syndrome: mechanisms, diagnosis and treatment

7 July 2018

1 reference

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Short QT syndrome. Genotype-phenotype correlations

7 July 2018

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Modulation of I(Kr) inactivation by mutation N588K in KCNH2: a link to arrhythmogenesis in short QT syndrome

7 July 2018

1 reference

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Cellular mechanisms underlying the development of catecholaminergic ventricular tachycardia.

7 July 2018

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A novel form of short QT syndrome (SQT3) is caused by a mutation in the KCNJ2 gene

7 July 2018

1 reference

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Short QT syndrome: pharmacological treatment

7 July 2018

1 reference

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Sudden death associated with short-QT syndrome linked to mutations in HERG.

7 July 2018

1 reference

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Short QT Syndrome: a familial cause of sudden death

7 July 2018

1 reference

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Effect of epicardial or biventricular pacing to prolong QT interval and increase transmural dispersion of repolarization: does resynchronization therapy pose a risk for patients predisposed to long QT or torsade de pointes?

7 July 2018

1 reference

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ECG phenomenon of idiopathic and paradoxical short QT intervals

7 July 2018

1 reference

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Novel potent human ether-a-go-go-related gene (hERG) potassium channel enhancers and their in vitro antiarrhythmic activity

7 July 2018

1 reference

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Short QT syndrome: successful prevention of sudden cardiac death in an adolescent by implantable cardioverter-defibrillator treatment for primary prophylaxis.

26 October 2018

1 reference

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Amplified transmural dispersion of repolarization as the basis for arrhythmogenesis in a canine ventricular-wedge model of short-QT syndrome

26 October 2018

1 reference

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Mutation in the KCNQ1 gene leading to the short QT-interval syndrome

26 October 2018

1 reference

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Epicardial activation of left ventricular wall prolongs QT interval and transmural dispersion of repolarization: implications for biventricular pacing

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2361425

Idiopathic short QT interval: a new clinical syndrome?

26 October 2018

1 reference

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Short QT syndrome--5 years of progress

9 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18362027

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.HRTHM.2008.01.022

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4 January 2020

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4 January 2020

PubMed publication ID

18362027

1 reference